FOMULATION AND EVALUATION OF GELATIN NANOPARTICLES FOR PULMONARY DRUG DELIVERY
Nitan Bharti*, S.L.Harikumar, Shishu, Abhishek Buddiraja
ABSTRACT
Pulmonary drug delivery is a non-invasive, non-systemic delivery
approach for both local and systemic drugs and a method to directly
target disorders of lung. The gelatin nanoparticles were prepared by
double desolvation method using different concentration of gelatin as
biodegradable polymer for lungs. The prepared gelatin nanoparticles
were evaluated for entrapment efficiency, particle size, polydispersity
index, zeta potential, transmission electron microscopy, in-vitro drug
release, stability study and in-vivo study. The entrapment efficiency of
all gelatin nanoparticles formulations were found to be in the range of
46.16 % - 58.60 %. The particle size of gelatin nanoparticle
formulations(GNps1, GNps2, GNps3, GNps4) were found to be 179.9 nm, 198.4 nm, 252.4
nm and 1545 nm,respectively. The gelatin nanoparticle formulation GNps3 was selected best
formulation depending upon the particle size less then 500nm and higher entrapment
efficiency as compared to GNps1 and GNps2. The zeta potential of gelatin nanoparticles
found to exhibit stability due to positive charge on the surface. The transmission electron
microscopy indicated the spherical surface of the gelatin nanoparticles. The in vitro release
was found to follow higuchi plot as compared to zero order plot, first order plot and
krosmeyer peppas plot. Stability studies showed that gelatin nanoparticle formulation GNps3
was stable when tested for particle size, entrapment efficiency and in vitro drug release at
refrigerated condition (5º±3ºC), at room temperature (25º±2ºC/65%±5% RH) and at accelerated condition (40º±2ºC/75%±5% RH) according to ICH guidelines for 6 months(180
days). In-vivo study using rat model indicated the localization gelatin nanoparticles in the
lungs of rat.
Keywords: Gelatin nanoparticles, pulmonary drug delivery, terbutaline sulfate, particle size, entrapment efficiency, stability.
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